CDKL5 deficiency disorder (CDD) is an early onset, neurodevelopmental syndrome
associated with pathogenic variants in the X-linked gene encoding cyclin-dependent kinase …

CDKL5 deficiency disorder (CDD) is an X-linked brain disorder of young children and is
caused by pathogenic variants in the cyclin-dependent kinase-like 5 (CDKL5) gene …

Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-linked
neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …

Cyclin-dependent kinase-like 5 (CDKL5) deficiency is a neurodevelopmental disorder
characterized by epileptic seizures, severe intellectual disability, and autistic features. Mice …

Cyclin‐dependent kinase‐like 5 (CDKL5, also known as STK9) is a serine/threonine protein
kinase originally identified in 1998 during a transcriptional mapping project of the human X …

Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene have been identified
in neurodevelopmental disorders including atypical Rett syndrome (RTT), autism spectrum …

Pathogenic mutations in cyclin-dependent kinase-like 5 (CDKL5) result in CDKL5 deficiency
disorder (CDD), a rare disease marked by early-life seizures, autistic behaviors, and …

CDKL5 disorder is a severe neurodevelopmental disorder caused by mutations in the X‐
linked CDKL5 (cyclin‐dependent kinase‐like five) gene. CDKL5 disorder primarily affects …

The X‐linked gene cyclin‐dependent kinase‐like 5 (CDKL5) encodes a serine/threonine
kinase abundantly expressed in the brain. Mutations in CDKL5 have been associated with …

Mutations in the X-linked CDKL5 (cyclin-dependent kinase-like 5) gene have been
associated with several forms of neurodevelopmental disorders, including atypical Rett …